Canonical Allele Identifier: CA500012346
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624483-G-T
MyVariant Identifiers: chr17:g.39780735G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624483G>T , CM000679.2:g.41624483G>T GRCh38
NC_000017.10:g.39780735G>T , CM000679.1:g.39780735G>T GRCh37
NC_000017.9:g.37034261G>T NCBI36
NG_008625.1:g.5148C>A
NG_009090.2:g.167230C>A , LRG_401:g.167230C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.27C>A MANE Select ENSP00000308452.8:p.Thr9=
ENST00000311208.12:c.27C>A ENSP00000308452.8:p.Thr9=
ENST00000463128.5:c.-313+260C>A ENSP00000468672.1:n.-313+260C>A
ENST00000491673.1:n.93C>A
ENST00000540235.5:c.-179C>A ENSP00000441751.2:n.-179C>A
NM_000422.2:c.27C>A NP_000413.1:p.Thr9=
NM_000422.3:c.27C>A MANE Select NP_000413.1:p.Thr9=
Search 100 bp 5'
Search 100 bp 3'